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在多甲藻素-叶绿素a-蛋白复合物中,激发能从离域S2激子高效转移的途径。

Efficient pathways of excitation energy transfer from delocalized S2 excitons in the peridinin-chlorophyll a-protein complex.

作者信息

Bricker William P, Lo Cynthia S

机构信息

Department of Energy, Environmental and Chemical Engineering, Washington University, St. Louis, Missouri 63130, United States.

出版信息

J Phys Chem B. 2015 May 7;119(18):5755-64. doi: 10.1021/jp511766j. Epub 2015 Apr 22.

Abstract

Excitation energy transfer (EET) in peridinin-chlorophyll-protein (PCP) complexes is dominated by the S1 → Qy pathway, but the high efficiencies cannot be solely explained by this one pathway. We postulate that EET from peridinin S2 excitons may also be important. We use complete active space configuration interaction calculations and the transition density cube method to calculate Coulombic couplings between peridinin and chlorophyll a in the PCP complex of the dinoflagellate Amphidinium carterae and compare monomeric and dimeric delocalized peridinin S2 excited states. Our calculations show that the S2 → Qy EET pathway from peridinin to chlorophyll a is the dominant energy transfer pathway from the S2 excited state in PCP, with several values in the sub-picosecond range. This result suggests that the S2 → Qy EET pathway may be responsible for the reported chlorophyll a bleaching signature seen in experiment at around 200 fs, and not the S2 → Qx pathway as previously suggested.

摘要

在多甲藻叶绿素蛋白(PCP)复合体中,激发能量转移(EET)主要由S1→Qy途径主导,但这种高效率不能仅用这一条途径来解释。我们推测来自多甲藻素S2激子的EET可能也很重要。我们使用完全活性空间组态相互作用计算和跃迁密度立方方法,来计算双鞭毛藻卡特亚得里亚海扁藻PCP复合体中多甲藻素与叶绿素a之间的库仑耦合,并比较单体和二聚体离域多甲藻素S2激发态。我们的计算表明,从多甲藻素到叶绿素a的S2→Qy EET途径是PCP中S2激发态的主要能量转移途径,有几个值处于亚皮秒范围内。这一结果表明,S2→Qy EET途径可能是实验中报道的在约200飞秒时出现的叶绿素a漂白特征的原因,而不是如先前所认为的S2→Qx途径。

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